FDA 510(k), K002571, MULITPLE MALE LATX CONDOM

FDA 510(k), K002571, MULITPLE MALE LATX CONDOM

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510(K) Number: K002571
Device Name: MULITPLE MALE LATX CONDOM
Manufacturer: PLEASURE LATEX PRODUCTS SDN. BHD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 08/18/2000
Decision Date: 11/16/2000
Regulation Medical Specialty: Obstetrics/Gynecology

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